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首页> 外文期刊>Fundamental & clinical pharmacology. >Influence of simulated weightlessness on the pharmacokinetics of acetaminophen administered by the oral route: a study in the rat.
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Influence of simulated weightlessness on the pharmacokinetics of acetaminophen administered by the oral route: a study in the rat.

机译:模拟失重对口服对乙酰氨基酚药代动力学的影响:一项在大鼠中的研究。

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摘要

During space flights, the human body is submitted to weightlessness which induces physiological variations that could modify drug disposition during space missions. Since space experiments are infrequent and difficult to perform, in order to evaluate pharmacokinetic modifications, simulation experiments of weightlessness have to be carried out on earth, using animal-models such as the Morey-Holton model. In this model, rats are suspended by the tail with their front paws on the ground. We studied the effects of simulated weightlessness on drug absorption and on gastric emptying, using acetaminophen as a probe. Three periods of suspension (1, 2 and 5 days) were compared with two control groups (free and attached rats). The attached group was used to evaluate a possible 'stress effect' caused by the suspension device. Each group was composed of 36 rats (12 sampling times and three rats per time). An oral dose of acetaminophen (100 mg/kg) was administered and blood samples were collected before and up to 12 h after administration. Plasma assays were performed using an high-performance liquid chromatography method with UV detection. The calculated population pharmacokinetic parameters were Ka, Kel (first order absorption and elimination constants) and Vd/F (apparent volume of distribution). The statistical interpretation of the population pharmacokinetic parameters indicated that 2 days of suspension significantly decreased the Vd/F by 83% and the Ka by 125%. The increase in the Ka was probably because of an increased acceleration of the gastric emptying and/or to a decrease in the total peripheral resistance which increased intestinal blood flow.
机译:在太空飞行期间,人体会失重,这会诱发生理变化,从而可能会在太空任务期间改变药物的处置方式。由于空间实验很少且难以执行,为了评估药代动力学修饰,必须使用诸如莫雷-霍顿(Morey-Holton)模型之类的动物模型在地球上进行失重模拟实验。在此模型中,大鼠的前爪在地面上,尾巴悬挂。我们使用对乙酰氨基酚作为探针,研究了模拟失重对药物吸收和胃排空的影响。将三个时期的悬架(1、2和5天)与两个对照组(自由和附着的大鼠)进行比较。附属小组被用来评估由悬挂装置引起的可能的“压力效应”。每组由36只大鼠组成(12次采样,每次3只)。口服对乙酰氨基酚(100 mg / kg),给药前和给药后12小时采集血样。使用高效液相色谱法和紫外线检测技术进行血浆检测。计算的群体药代动力学参数为Ka,Kel(一级吸收和消除常数)和Vd / F(表观分布体积)。群体药代动力学参数的统计解释表明,悬浮2天后,Vd / F明显降低了83%,Ka降低了125%。 Ka的增加可能是由于胃排空的加快和/或总外周阻力的降低,这增加了肠血流量。

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